Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chromic Acid | HCID 24425 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 54283188 | HCID 54283188 | — |
| Catalyst | Methanol | HCID 887 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 21505611 | HCID 21505611 | — |
Reaction Steps
A 1.65 g. portion of 3,6-dihydro-α-(p-fluorophenyl)- 4-(3-methyl-5-isoxazolyl)-1(2H)-pyridine butanol, prepared as described in Example 10, in 35 ml. of acetic acid is stirred at room temperature. A 30 ml. portion of chromic acid in acetic acid (prepared by dissolving 1.1 gm. of chromium oxide in 50 ml. of acetic acid and 10 ml. of water) is added dropwise and the mixture is stirred for 3 hours and then allowed to stand overnight. A few drops of methanol are added and sufficient solid sodium bicarbonate to neutralize the solution. Water is also added. The mixture is extracted 3 times with ether. The extracts are dried over magnesium sulfate, filtered and evaporated yielding a pink solid which is recrystallized twice from methanol, m.p. 96°-98° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03985754 |
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| Source dataset | uspto-grants-1976_10 |
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| ORD ID | ord-54928926231d4a959191b15d215ae6d0 |
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| Source note | uspto-grants-1976_10 |
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